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Over the past decade, international efforts have greatly increased the number of people in developing countries receiving antiretroviral therapy to treat HIV/AIDS. Today, more than 8 million people receive therapy, although more than 34 million people are living with HIV.
Viread® (tenofovir disoproxil fumarate) and Truvada® (emtricitabine/tenofovir disoproxil fumarate) are recommended by the World Health Organization as components of antiretroviral therapy. We make these medicines available in low- and middle-income countries through two means:
Our single tablet regimens Atripla® (efavirenz/emtricitabine/tenofovir disoproxil fumarate) and Complera® (emtricitabine/rilpivirine/tenofovir disoproxil fumarate) were developed and are distributed through joint ventures with Merck and Janssen Therapeutics, respectively. We work with these companies to manage access for developing countries.
Also, as new HIV medicines advance through the research and development pipeline, we take steps to introduce them through access programs. For example, in July 2011 Gilead extended licenses to Indian partners to grant them future rights to produce generic versions of our newest single tablet regimen, Stribild® (elvitegravir 150 mg/cobicistat 150 mg/emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg). This was done prior to Stribild's approval by the U.S. Food and Drug Administration in August 2012.